Biological invasions pose a threat to nearly every ecosystem worldwide.1,2 Although eradication programs can successfully eliminate invasive species and enhance native biodiversity, especially on islands,3 the effects of eradication on cross-ecosystem processes are unknown. On islands where rats were never introduced, seabirds transfer nutrients from pelagic to terrestrial and nearshore marine habitats, which in turn enhance the productivity, biomass, and functioning of recipient ecosystems.4-6 Here, we test whether rat eradication restores seabird populations, their nutrient subsidies, and some of their associated benefits for ecosystem function to tropical islands and adjacent coral reefs. By comparing islands with different rat invasion histories, we found a clear hierarchy whereby seabird biomass, seabird-driven nitrogen inputs, and the incorporation of seabird-derived nutrients into terrestrial and marine food chains were highest on islands where rats were never introduced, intermediate on islands where rats were eradicated 4-16 years earlier, and lowest on islands with invasive rats still present. Seabird-derived nutrients diminished from land to sea and with increasing distance to rat-eradicated islands, but extended at least 300 m from shore. Although rat eradication enhanced seabird-derived nutrients in soil, leaves, marine algae, and herbivorous reef fish, reef fish growth was similar around rat-eradicated and rat-infested islands. Given that the loss of nutrient subsidies is of global concern,7 that removal of invasive species restores previously lost nutrient pathways over relatively short timescales is promising. However, the full return of cross-ecosystem nutrient subsidies and all of their associated demographic benefits may take multiple decades.Semantic memory-general knowledge of ideas and concepts-includes generalization processes that support inference. https://www.selleckchem.com/products/abt-199.html Episodic memory, on the other hand, preserves the specificity of individual events by binding together unique combinations of elements from an episode and relies on pattern separation to distinguish similar experiences. These two memory systems play complementary roles, supporting different mnemonic goals, but the nature and extent of their interdependence is unclear.1,2 Some models suggest that new information is encoded initially as hippocampus-dependent episodic memory and then, either through repetition or gist extraction, becomes semantic over time.3,4 These models also posit a neocortical route to semantic memory acquisition exists that can bypass the hippocampus.3 Both proposed routes are slow learning mechanisms, yet generalization can occur rapidly. Recent models suggest that fast generalization relies, in part, on the retrieval of individual but related episodes.5,6 Such episodic memory gating mechanisms render fast generalization contingent on the memory specificity of instances, a pattern that has been observed in adults.7,8 None of these models take into account the observation that generalization and episodic specificity have asynchronous developmental profiles, with generalization emerging years before episodic memory.9,10 We ask two questions about generalized and specific memory during early childhood first, is rapid generalization contingent on remembering specific past memories? And second, does the strength or nature of this contingency differ across development? We found that the interdependence of generalization and episodic memory varies across development generalization success in adults, but not in children, was contingent on context binding.Although gene duplication is an important source of evolutionary innovation, the functional divergence of duplicates can be opposed by ongoing gene conversion between them. Here, we report on the evolution of a tandem duplication of Na+,K+-ATPase subunit α1 (ATP1A1) shared by frogs in the genus Leptodactylus, a group of species that feeds on toxic toads. One ATP1A1 paralog evolved resistance to toad toxins although the other retained ancestral susceptibility. Within species, frequent non-allelic gene conversion homogenized most of the sequence between the two copies but was counteracted by strong selection on 12 amino acid substitutions that distinguish the two paralogs. Protein-engineering experiments show that two of these substitutions substantially increase toxin resistance, whereas the additional 10 mitigate their deleterious effects on ATPase activity. Our results reveal how examination of neo-functionalized gene duplicate evolution can help pinpoint key functional substitutions and interactions with the genetic backgrounds on which they arise.To evaluate the stability and resilience1 of coastal ecosystem communities to perturbations that occurred during the Anthropocene,2 pre-industrial biodiversity baselines inferred from paleoarchives are needed.3,4 The study of ancient DNA (aDNA) from sediments (sedaDNA)5 has provided valuable information about past dynamics of microbial species6-8 and communities9-18 in relation to ecosystem variations. Shifts in planktonic protist communities might significantly affect marine ecosystems through cascading effects,19-21 and therefore the analysis of this compartment is essential for the assessment of ecosystem variations. Here, sediment cores collected from different sites of the Bay of Brest (northeast Atlantic, France) allowed ca. 1,400 years of retrospective analyses of the effects of human pollution on marine protists. Comparison of sedaDNA extractions and metabarcoding analyses with different barcode regions (V4 and V7 18S rDNA) revealed that protist assemblages in ancient sediments are mainly composed of species known to produce resting stages. Heavy-metal pollution traces in sediments were ascribed to the World War II period and coincided with community shifts within dinoflagellates and stramenopiles. After the war and especially from the 1980s to 1990s, protist genera shifts followed chronic contaminations of agricultural origin. Community composition reconstruction over time showed that there was no recovery to a Middle Ages baseline composition. This demonstrates the irreversibility of the observed shifts after the cumulative effect of war and agricultural pollutions. Developing a paleoecological approach, this study highlights how human contaminations irreversibly affect marine microbial compartments, which contributes to the debate on coastal ecosystem preservation and restoration.